Device for Minimally Invasive Delivery of Treatment Substance

ABSTRACT

Systems, methods, and devices for delivering ablation fluid to a location of interest within a body (e.g., a location with the lung) are described herein. Ablation fluid delivery systems and devices can include flexible delivery needles within which a plurality of smaller flexible needles is housed. The smaller flexible needles can be configured to articulate or bend with respect to the flexible delivery needle to increase an effective delivery area for the ablation fluid. The smaller flexible needles can include apertures or other openings to facilitate delivery of the ablation fluid to the location of interest.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to and the benefit of U.S. provisionalpatent application Ser. No. 61/779,483 filed on Mar. 13, 2013 entitled“Device for Minimally Invasive Delivery of Treatment Substance,” theentire disclosure of which is hereby incorporated by reference as if setforth in its entirety for all purposes.

BACKGROUND

1. Technical Field

Embodiments of the invention relate generally to the field of medicaldevices, and in particular, to methods, systems, and devices fornavigating to and delivering chemicals or other substances to tissuesuch as lung nodules or other sites of interest. In particular, certainembodiments described herein use a flexible delivery needle withinternal flexible needles to deliver substances to a site of interestwithin the body.

2. Description of the Related Art

Early diagnosis of potentially cancerous tissue is an important step inthe treatment of cancer because, the sooner that cancerous tissue can betreated, and the better the patient's chances are for survival. Typicaldiagnostic procedures involve biopsying tissue at a site of interest. Inthe case of lungs, lung cancer can be difficult to diagnose due to thedifficulties in accessing airways near areas of interest. Areas ofinterest may present as lung nodules small tissue masses in the lungthat may range in size between 0.5-30 mm—that typically are biopsied toascertain whether the tissue therein is cancerous or otherwise diseased.In some instances treatment of tissue in an area of interest can includedelivery of chemicals (e.g., ablative chemicals) or other substances.

Existing systems typically are constrained by difficulties in accessinglung nodules, especially in the smaller peripheral airways that may betoo narrow to accommodate larger catheters and biopsy/substance deliveryapparatuses. Further, the biopsy/substance delivery needles normally arestraight and relatively inflexible. Thus, the biopsy/substance deliveryneedles can limit the articulation of a bronchoscope or can be difficultto pass through a working channel of a bronchoscope when thebronchoscope is articulated around a tight corner. In some instances,the material of the needle may inelastically yield, which can result ina bent needle that is difficult to control. In addition, the straightbiopsy needles obtain samples along an axis of the needle through backand forth cycling of the needle. Thus, obtaining multiple samples fromdifferent regions of a single nodule, for example, can be difficult andcan require repeated repositioning of the bronchoscope or guide sheath,for example. Furthermore, delivery of substances to different regions ofa single nodule can be difficult.

SUMMARY

Accordingly, embodiments described herein relate generally to methods,systems, and devices for navigating to and biopsying tissue at a site ofinterest. In particular, embodiments described herein may be used forbiopsying tissue in a lung (such as lung nodules or lymph nodes) using aflexible transbronchial biopsy aspiration needle system. Certainembodiments provide for the flexible biopsy needle to be steerable orguidable to a location of interest. Further embodiments provide for avisualization system (e.g., ultrasound) to be provided in a flexible,miniaturized configuration, and this visualization system may becombined with the flexible biopsy needle.

In one embodiment, a system for obtaining a tissue sample in or near anairway comprises:

a flexible needle with distal and proximal ends, the distal end of theneedle comprising a less flexible distal tip region and a more flexibleproximal region, the less flexible distal tip region comprising apiercing tip configured to obtain a tissue sample, and the more flexibleproximal region configured to bend;

a catheter, wherein the catheter comprises at least one interior lumen,the flexible needle being slidably received within the at least oneinterior lumen; and

a suction source in fluid communication with the flexible needle.

Additional embodiments comprise a steering mechanism configured to steerthe flexible needle toward a site of the tissue to be sampled. Thesteering mechanism may comprise at least one guidewire extendinglongitudinally along the exterior of the flexible needle or the at leastone interior lumen. In some configurations, the steering mechanism maycomprise a guidewire extending within an interior lumen of the flexibleneedle. In some embodiments, the guidewire is removable from theinterior lumen of the flexible needle. The system may also comprise anavigation system. The navigation system can utilize an ultrasoundprobe. In some embodiments, the ultrasound probe is located at a distalend of the catheter. In some embodiments, the catheter comprises asecond lumen and the ultrasound probe is received within the secondlumen. In some embodiments, the catheter is received within the workingchannel of a bronchoscope. Some configurations may provide for thecatheter being received within a bronchoscope comprising a secondsteering mechanism, wherein the second steering mechanism can steerindependently of the steering mechanism configured to steer the flexibleneedle.

In another embodiment, a method for obtaining a tissue sample in or nearan airway comprises:

identifying a location in the airway in close proximity to a tissuesample site;

introducing a flexible needle into the airway;

navigating the flexible needle to the location in the airway;

articulating the flexible needle in a direction toward a tissue samplesite; and

obtaining a tissue sample from the tissue sample site, wherein theflexible needle pierces into the tissue sample site, and wherein suctionis applied to the flexible needle so as to collect tissue from thetissue sample site.

In some embodiments, the flexible needle is articulated by a steeringmechanism. In some embodiments, the flexible needle is inserted into alumen of a catheter. In some embodiments, the step of navigatingcomprises locating the flexible needle with a radioopaque markersituated on the flexible needle and/or the catheter. In someembodiments, the flexible needle is inserted into a lumen of abronchoscope.

In some embodiments, a flexible needle configured to access a locationnear an airway, has a length and comprises a proximal end and a distalend comprising a piercing tip. The needle can include a flexibleproximal tip region located along the length of the flexible needlebetween the distal end and the proximal end, the flexible proximal tipregion having one or more flexibility increasing features and configuredto bend. In some embodiments, the flexible needle includes a flexibledistal tip region located along the length of the flexible needlebetween the flexible proximal tip region and the distal end, wherein theflexible distal tip region is less flexible than the proximal tipregion. The flexibility increasing feature can be, for example, one ormore cuts in the flexible needle. In some embodiments, the one or morecuts extend in a spiral fashion along flexible proximal tip region. Insome embodiments, the one or more cuts are arranged in a jigsawconfiguration. In some embodiments, the one or more cuts are arranged ina serpentine configuration. In some embodiments, the one or more cutscomprise an interrupted spiral pattern where the flexible needle has cutand uncut portions along a same spiral path. In some embodiments, theone or more cuts are distributed asymmetrically on a portion of thelength of flexible needle such that the cuts are located on only aportion of a radial circumference of the flexible needle.

According to some embodiments, the flexible needle and any variantsthereof can be used in combination with a catheter comprising at leastone interior lumen, the flexible needle being slidably received withinthe at least one interior lumen, and with a suction source in fluidcommunication with the flexible needle. Such a combination can form asystem for accessing tissue near an airway. The system can include asteering mechanism configured to steer the flexible needle toward thetissue sample site. In some embodiments, the steering mechanismcomprises at least one guidewire extending longitudinally along theexterior of the flexible needle or the at least one interior lumen. Insome embodiments, the steering mechanism comprises a guidewire extendingwithin an interior lumen of the flexible needle. In some embodiments,the guidewire is removable from the interior lumen of the flexibleneedle. According to some variants, the system includes a navigationsystem. The navigation system can be an ultrasound probe. The ultrasoundprobe can be located at a distal end of the catheter. The catheter caninclude a second lumen and the ultrasound probe is received within thesecond lumen. In some embodiments, the catheter is received within theworking channel of a bronchoscope. In some embodiments, the catheter isreceived within a bronchoscope comprising a second steering mechanism,and the second steering mechanism can steer independently of thesteering mechanism configured to steer the flexible needle.

In some embodiments, a method of manufacturing a flexible needle caninclude providing a tube shaped length of resilient material having adistal end and a proximal end, forming an angled tip on the distal endof the tube shaped length of resilient material, and forming one or moreflexibility increasing features on the tube shaped length of resilientmaterial, such that the flexible needle has a flexible proximal tipregion located along the tube shaped length of resilient materialbetween the distal end and the proximal end, the flexible proximal tipregion having one or more flexibility increasing features and configuredto bend, and such that a flexible distal tip region located along thetube shaped length of resilient material between the flexible proximaltip region and the distal end, wherein the flexible distal tip region isless flexible than the proximal tip region. In some embodiments, formingthe one or more flexibility increasing features includes cutting one ormore cuts into a wall of the tube shaped length of resilient material.In some embodiments, cutting the one or more cuts includes water jettingthe wall of the tube shaped length of resilient material. In someembodiments, cutting the one or more cuts includes laser cutting thewall of the tube shaped length of resilient material. In someembodiments, cutting the one or more cuts includes chemical etching thewall of the tube shaped length of resilient material.

A method for obtaining a tissue sample near an airway can includeidentifying a location in the airway in close proximity to a tissuesample site, introducing a flexible needle into the airway, navigatingthe flexible needle to the location in the airway, articulating theflexible needle in a direction toward the tissue sample site, andobtaining a tissue sample from the tissue sample site, wherein theflexible needle pierces the airway and into the tissue sample site, andwherein suction is applied to the flexible needle so as to collecttissue from the tissue sample site. The method can include articulatingthe flexible needle using a steering mechanism. In some embodiments, theflexible needle is inserted into a lumen of a catheter. In someembodiments, the step of navigating comprises locating the flexibleneedle with a radioopaque marker situated on the flexible needle and/orthe catheter. In some embodiments the flexible needle is inserted into alumen of a bronchoscope.

Various example embodiments of the disclosure can be described in viewof the following clauses:

Clause 1: a flexible needle configured to access a location near anairway, the flexible needle having a length and comprising: a proximalend; a distal end comprising a piercing tip; a flexible proximal tipregion located along the length of the flexible needle between thedistal end and the proximal end, the flexible proximal tip region havingone or more flexibility increasing features and configured to bend; anda flexible distal tip region located along the length of the flexibleneedle between the flexible proximal tip region and the distal end,wherein the flexible distal tip region is less flexible than theproximal tip region.

Clause 2: the flexible needle of Clause 1, wherein the flexibilityincreasing feature comprises one or more cuts in the flexible needle.

Clause 3: the flexible needle of Clause 2, wherein the one or more cutsextend in a spiral fashion along flexible proximal tip region.

Clause 4: the flexible needle of Clause 2, wherein the one or more cutsare arranged in a jigsaw configuration.

Clause 5: the flexible needle of Clause 2, wherein the one or more cutsare arranged in a serpentine configuration.

Clause 6: the flexible needle of Clause 2, wherein the one or more cutsare arranged in an interrupted spiral pattern where the flexible needlehas cut and uncut portions along a same spiral path.

Clause 7: the flexible needle of and of Clauses 2-6, wherein the one ormore cuts are distributed asymmetrically on a portion of the length offlexible needle such that the cuts are located on only a portion of aradial circumference of the flexible needle.

Clause 8: a system for accessing tissue near an airway, the systemcomprising: the flexible needle of Clause 1; a catheter comprising atleast one interior lumen, the flexible needle being slidably receivedwithin the at least one interior lumen; and a suction source in fluidcommunication with the flexible needle.

Clause 9: the system of Clause 8, further comprising a steeringmechanism configured to steer the flexible needle toward the tissuesample site.

Clause 10: the system of Clause 9, wherein the steering mechanismcomprises at least one guidewire extending longitudinally along theexterior of the flexible needle or the at least one interior lumen.

Clause 11: the system of either of Clauses 9 or 10, wherein the steeringmechanism comprises a guidewire extending within an interior lumen ofthe flexible needle.

Clause 12: the system of Clause 11, wherein the guidewire is removablefrom the interior lumen of the flexible needle.

Clause 13: the system of any of Clauses 8-12, further comprising anavigation system.

Clause 14: the system of Clause 13, wherein the navigation system is anultrasound probe.

Clause 15: the system of Clause 14, wherein the ultrasound probe islocated at a distal end of the catheter.

Clause 16: the system of Clauses 14 or 15, wherein the cathetercomprises a second lumen and the ultrasound probe is received within thesecond lumen.

Clause 17: the system of any of Clauses 8-16, wherein the catheter isreceived within the working channel of a bronchoscope.

Clause 18: the system of any of Clauses 9-17, wherein the catheter isreceived within a bronchoscope comprising a second steering mechanism,and wherein the second steering mechanism can steer independently of thesteering mechanism configured to steer the flexible needle.

Clause 19: a method of manufacturing a flexible needle comprising:providing a tube shaped length of resilient material having a distal endand a proximal end; forming an angled tip on the distal end of the tubeshaped length of resilient material; forming one or more flexibilityincreasing features on the tube shaped length of resilient material,such that the flexible needle comprises: a flexible proximal tip regionlocated along the tube shaped length of resilient material between thedistal end and the proximal end, the flexible proximal tip region havingone or more flexibility increasing features and configured to bend; anda flexible distal tip region located along the tube shaped length ofresilient material between the flexible proximal tip region and thedistal end, wherein the flexible distal tip region is less flexible thanthe proximal tip region.

Clause 20: the method of Clause 19, wherein forming the one or moreflexibility increasing features includes cutting one or more cuts into awall of the tube shaped length of resilient material.

Clause 21: the method of Clause 20, wherein cutting the one or more cutsincludes water jetting the wall of the tube shaped length of resilientmaterial.

Clause 22: the method of Clause 20, wherein cutting the one or more cutsincludes laser cutting the wall of the tube shaped length of resilientmaterial.

Clause 23: the method of Clause 20, wherein cutting the one or more cutsincludes chemical etching the wall of the tube shaped length ofresilient material.

Clause 24: a method for obtaining a tissue sample near an airway, themethod comprising: identifying a location in the airway in closeproximity to a tissue sample site; introducing a flexible needle intothe airway; navigating the flexible needle to the location in theairway; articulating the flexible needle in a direction toward thetissue sample site; and obtaining a tissue sample from the tissue samplesite, wherein the flexible needle pierces the airway and into the tissuesample site, and wherein suction is applied to the flexible needle so asto collect tissue from the tissue sample site.

Clause 25: the method of Clause 24, wherein the flexible needle isarticulated by a steering mechanism.

Clause 26: the method of any of Clauses 24 or 25, wherein the flexibleneedle is inserted into a lumen of a catheter.

Clause 27: the method of Clause 26Error! Reference source not found.,wherein the step of navigating comprises locating the flexible needlewith a radioopaque marker situated on the flexible needle and/or thecatheter.

Clause 28: the method of Clause 24, wherein the flexible needle isinserted into a lumen of a bronchoscope.

A needle assembly for delivery a treatment substance to a site withinthe body can comprise: a delivery needle defining a delivery lumen andhaving a delivery needle wall, a proximal end, and a distal end, thedelivery needle wall having one or more cut patterns to increase theflexibility of the delivery needle; a plurality of internal needles,each internal needle defining an internal needle lumen and having aninternal needle wall, a proximal end, and a distal end, the plurality ofneedles configured to transition between a contracted position and anexpanded position; and a treatment substance source in fluidcommunication with the internal needle lumens of the plurality ofinternal needles; wherein each of the plurality of internal needles isconfigured to extend in a distal direction and flare outward from thedistal end of the delivery needle when in the extend position andwherein the plurality of internal needles are housed within the deliverylumen when the contracted position. In some embodiments, an internalsurface of the delivery needle wall is coated with a substanceconfigured to reduce or eliminate the likelihood that the internalneedles will stick to or catch on the delivery needle wall when theinternal needles are transitioned between the contracted position andthe expanded position. In some embodiments, the internal needles wallsof the internal needles include cut features, the cut featuresfacilitating fluid communication between the internal needle lumen andan exterior of the internal needles. According to some variants, theneedle assembly comprises a flexible shaft having a distal end and aproximal end, the distal end of the flexible shaft coupled with theproximal ends of the internal needles. In some embodiments, the needleassembly comprises three internal needles. In some embodiments, each ofthe internal needles had a distal aperture in fluid communication withthe internal needle lumen. The distal ends of the internal needles canbe sharpened and/or beveled. The distal end of the delivery needle canbe sharpened and/or beveled.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other features, aspects and advantages of the presentdisclosure are described in detail below with reference to the drawingsof various embodiments, which are intended to illustrate and not tolimit the disclosure. The drawings comprise the following figures inwhich;

FIG. 1 is a perspective view of a transbronchial needle aspirationsystem comprising an ultrasound sensor.

FIG. 2 illustrates a side view of an embodiment of a flexible needle.

FIGS. 3A-G illustrate various configurations for interruptions that maybe made along one or more portions of embodiments of the flexibleneedles.

FIG. 4 illustrates a close-up view of the flexible shaft portion of anembodiment of a flexible needle.

FIG. 5 illustrates a side view of another embodiment of the flexibleneedle.

FIGS. 6A-D illustrate schematic cross-section views of differentembodiments of a steerable, flexible needle assembly.

FIG. 7 illustrates a side view of an embodiment of a steerable, flexibleneedle assembly.

FIG. 8 illustrates an embodiment of a steerable, flexible needleassembly comprising an inner guidewire.

FIG. 9 illustrates the proximal end of an embodiment of a flexibleneedle assembly comprising an inner guidewire.

FIG. 10 is a fluoroscopy image of an embodiment of a flexible needlewith an inner guidewire.

FIGS. 11A-B illustrate front and side cross sectional views of anembodiment of a multi-lumen, steerable catheter in a relaxed state. FIG.11C illustrates a side cross sectional view of the catheter in anarticulated state.

FIGS. 12A-C are illustrations of a bronchoscope showing various degreesof articulation achievable without any biopsy needle, with aconventional straight biopsy needle, and with an embodiment of aflexible biopsy needle.

FIGS. 13A-C are illustrations of an embodiment of a flexible needle withsteering wires.

FIGS. 14A-B are illustrations of an embodiment of a flexible needleinserted into a multi-lumen, steerable catheter.

FIGS. 15A-C are illustrations of a bronchoscope comprising an ultrasoundprobe and showing various degrees of articulation achievable without anybiopsy needle, with a conventional straight biopsy needle, and with anembodiment of a flexible biopsy needle.

FIGS. 16A-C are illustrations of an embodiment of a flexible needle.

FIG. 17 is an illustration of a handle that may be used to manipulateand control embodiments of the flexible needles described herein.

FIG. 18 is an illustration of an embodiment of a flexible needle showingthe distal tip thereof.

FIG. 19 is a fluoroscopy image of an embodiment of a flexible needlewith an inner guidewire.

FIG. 20A is a partial cross-section view of a delivery needle in whichone or more internal needles are positioned.

FIG. 20B is an elevated end view of the delivery needle of FIG. 20A fromthe viewing plane 20B-20B of FIG. 20A.

FIG. 21A is a partial cross-section view of the delivery needle of FIG.20A wherein the one or more internal needles are deployed outside of thedelivery needle.

FIG. 21B is an elevated end view of the delivery needle and one or moredeployed internal needles of FIG. 21A from the viewing plane 21B-21B ofFIG. 21A.

FIG. 22A illustrates a delivery needle in communication with an area ofinterest within the body.

FIG. 22B illustrates a delivery needle with deployed internal flexibleneedles in communication with an area of interest within the body.

FIG. 23A illustrates an isometric view of a delivery needle with aspiral scribe on the distal tip, which may be used to reflect ultrasoundwaves.

FIG. 23B illustrates a side view of a delivery needle with a spiralscribe on the distal tip, which may be used to reflect ultrasound waves.

DETAILED DESCRIPTION

Various embodiments of a flexible transbronchial needle aspirationsystem, a minimally invasive substance delivery system, and theirrelated components and parts will now be described with reference to theaccompanying figures. The terminology used in the description presentedherein is not intended to be interpreted in any limited or restrictedmanner. Rather, the terminology is simply being utilized in conjunctionwith a detailed description of embodiments of the systems, methods andrelated components. Furthermore, embodiments may comprise several novelfeatures, no single one of which is solely responsible for its desirableattributes or is believed to be essential to practicing the disclosureherein described. For example, while references may be made herein tousing the embodiments described herein with terms such as “lung,”“airway,” “nodule,” and so forth, these terms are broad and theembodiments described may be used without limitation and unlessotherwise indicated can be used to access to other vessels, passages,lumens, body cavities, tissues, and organs present in humans andanimals. For example, lumens such as the gastrointestinal system may beaccessed with the embodiments described herein.

Presently, various companies offer products directed to transbronchialneedle aspiration systems, some of which include visualization systemsto direct the needle to a site to be biopsied. For example, Olympusmanufactures an ultrasound system (the Endobronchial UltrasoundTransbronchial Needle Aspiration system (EBUS-TBNA)) substantially asillustrated in FIG. 1. As shown, the system 100 employs an ultrasoundprobe 102 situated at the distal end of a specialized bronchoscope 106.A rigid needle 104 extends at an angle from an aperture 108. The needle104 is sheathed prior to deployment by a catheter or sheath 110 thatcontains coils 112. The coils 112 preferably surround the needle 104 toreduce the likelihood of the needle 104 perforating a working channel ofthe bronchoscope 106. Because the needle 104 is rigid and its range ofmotion constrained, the system 100 is limited in the area of tissue thatcan be easily biopsied. Although some medical practitioners mayoccasionally bend needles similar to the needle 104 so as to be able tobiopsy tissue at larger angles relative to the axis of the bronchoscope,these needles remain rigid (albeit bent) and still limit the area oftissue that can be biopsied.

FIG. 2 illustrates an embodiment of a flexible needle 200. As will bediscussed, embodiments of this flexible needle 200, as well as the otherembodiments described herein, may be used in conjunction with existingsystems and methods (such as the system 100 illustrated in FIG. 1) forlocating, navigating to, and biopsying regions (e.g., lung nodules,lymph nodes) of interest. Use of a flexible needle can permit biopsyingtissue and cells in a much larger area and over a wider range of anglescompared to existing systems, and certain embodiments allow for greaterarticulation of a bronchoscope or endoscope so as to gain access totortuous areas of the anatomy. Accordingly, the use of such embodimentscan provide increased sample quality, greater diagnostic yields, and areduction of erroneous diagnostic results (e.g., false positives ornegatives). It will be noted that although bronchoscopes are referred toherein, other endoscopes may be usable (e.g., gastric endoscopes,colonoscopes). As such, other lumens may be explored, navigated to, andbiopsied using the embodiments described herein.

A proximal end of the needle 200 comprises a proximal shaft portion 202.The distal end comprises a flexible shaft portion 204 that is moreflexible than the proximal shaft portion and preferably able toselectively bend, curve, and articulate such that the respective ends ofthe needle 200 are not necessarily collinear. Flexible shaft portion 204may be provided with a laser cut feature, for example a spiral cut, toimprove the flexibility in this region. For example, due to the flexiblenature of the needle 200, the needle 200 is capable of at least twodifferent deflections in radial directions to angles that would exceedthe yield strength of a solid needle formed of the same material. At theextreme distal end, the flexible shaft portion 204 comprises a shortdistal tip portion 206. This distal tip portion 206 is configured with apiercing tip used to obtain biopsy cell and/or tissue samples. Thedistal tip portion 206 preferably is more rigid than the flexible shaftportion 204. It is contemplated that the needle is formed unitarily of asingle material.

In some embodiments, the flexible transbronchial needle 200 can beadvanced to peripheral airways and can easily penetrate into the lungparenchyma. In a preferred configuration, the needle 200 can penetratetissue at a depth of at least 15 mm. In some embodiments, the distal end204, 206 of the needle 200 can articulate such that it can bend over 90degrees relative to a more proximal portion. In a preferred embodimentand when inserted into a bronchoscope working channel (such as theBF-P180™ bronchoscope manufactured by Olympus), the needle 200 canarticulate at least 130 degrees when the needle tip 206 is flush withthe end of the bronchoscope. When inserted into a system 100 similar tothat illustrated in FIG. 1, embodiments of the needle 200 can articulateapproximately 110 degrees. Due to its relatively low-profileconstruction, embodiments of the flexible needle 200 may beminiaturized, in conjunction with a catheter or guide sheath, so as tofit into working channels (e.g., of a bronchoscope) that are as small asor smaller than 2.0 mm. For example, certain embodiments of the needle200 can be used with small guide sheaths with a minimum inner diameterof 0.7 mm.

The flexible needle 200 can be formed from any suitable material. Insome configurations, the flexible needle 200 may be formed from a metalor metal alloy, such as stainless steel, nitinol or the like. In somearrangements, the flexible needle 200 can comprise a polymer or othersuitable covering over at least a portion of the length of the flexibleneedle 200. In some configurations, the flexible needle 200 can comprisea heat shrink material that covers substantially the entire length ofthe flexible needle 200. In some configurations, one or more of theinner and outer surfaces can receive a coating of any suitable material.The coating can improve the lubricity of the coated surface or increasethe smoothness of the coated surface. In some configurations, theflexible needle 200 is constructed from a hypotube. Preferably, thehypotube is constructed to be relatively smooth along at least aproximal portion such that when introduced into a device such as acatheter lumen, for example but without limitation, the hypotube is ableto relatively freely slide, rotate, or otherwise move along the lumen.

Embodiments described herein (for example but without limitation, theembodiment illustrated in FIG. 2) may be used with any suitablevisualization device, such as the ultrasound system 100 of FIG. 1,navigation system or the like. By using the flexible transbronchialneedle 200, access to regions of interest in the lung or in othertissues can be easier and more straightforward, because the flexibleneedle 200 is able to articulate, bend, and/or curve to a greater degreethan a straight, inflexible needle, and independently from the angle orarticulation that a bronchoscope or endoscope may have at the same time.This may, for example, enable biopsying of tissue at an angle close toperpendicular from the bronchoscope. In addition, the flexible needle200 can bend in a region between the distal piecing tip 206 and thedistal end of any protective guide sheath or catheter. Further, thecoils 112 present in the sheath 110 of the existing system 100 can bemade shorter or eliminated entirely due to the flexibility of theneedle. In other words, the flexibility of the distal portion 204 of theflexible needle 200 reduces the likelihood of perforating the workingchannel of the bronchoscope. The increased flexibility also decreasesthe radial forces exerted by the distal tip 206 of the needle 200 duringnavigation through the working channel of the bronchoscope, for examplebut without limitation.

In some embodiments, visualization of the needle 200 may be enhanced (inparticular for ultrasound) by including signature markers 2059 that willenhance the visibility of the needle 200, particularly at the distaltip. Signature markers may include forming dimples, scallops, a spiralscribe which may be laser cut, or the like on the needle 200, whichdimples, scallops, a spiral scribe which may be laser cut, or the likecan reflect ultrasound. Such features provide echogenic surface fordetection by ultrasound. Of course, other markers visible for differentvisualization methods can be used, such as radioopaque markers locatedon various elements of the catheter or sheath used to deploy the needle200, as well as the needle 200 itself.

Although ultrasound has been found to be a preferable system forvisualization due to the relatively high penetration depth (10-18 mm) ofultrasound, other systems also may be used. In some configurations, aspiral ultrasound probe can be used to provide improved visualizationover an ultrasound probe that provides visualization in only a singleplane. Other systems for locating and navigating to tissues of interest,such as lung nodules and lymph nodes, may include using a bronchoscopewith an optical channel, fluoroscopy, optical coherence tomography, andmagnetic resonance imaging. Any other suitable navigation systems alsocan be used, including commercial systems using X-ray computedtomography assisted visualization (such as, for example but withoutlimitation, the Bf Navi™ system sold by Olympus and the i-Logic™ systemsold by SuperDimension).

FIGS. 3A-G illustrate various configurations for flexibility increasingfeatures (e.g., slots, openings, or grooves) that may be formed alongvarious regions of transbronchial needles to increase flexibility. Forexample, such flexibility increasing features may be made into theflexible shaft portion 204 of FIG. 2. Generally, one or more flexibilityincreasing features, or cut patterns, 304 such as cuts for example butwithout limitation, may be made onto the needle wall 300 of the needle;these cuts 304 may then define one or more regions of increasedflexibility 302. These cuts 304 permit the region of increasedflexibility 302 on the flexible shaft portion to selectively articulateand bend more easily and to a greater degree than an equivalent portionthat is uncut, thereby permitting navigation and biopsying of tissue intortuous regions of, for example, an airway, that may not be possibleusing a traditional rigid needle.

The flexibility of the region of increased flexibility 302 may betailored as desired for a particular application. The flexibility can bechanged, for example, by modifying the thickness of the needle wall 300,the materials used therein, and the spacing, pitch, and angle betweenthe flexibility increasing features 304 in the region of increasedflexibility 302. Preferably, the cuts 304 extend in a spiral fashionalong the region of increased flexibility 302. In preferred embodiments,the features 304 are cut with a thickness between about 0.0010 and about0.0025 inches, and even more preferably a range between about 0.0015 andabout 0.0020 inches.

Additionally, the region of increased flexibility 302 does not need tohave features such as the single pitch illustrated in FIG. 3A, but, withreference to FIG. 3B, can instead have features that are of a variablepitch, wherein the spacing or pitch can be changed in a continuous orstepwise fashion, for example but without limitation. Additionally,although the cuts shown in these figures are made in a continuous andsingle cut, high flexibility regions may be made using one or morediscontinuous cuts. In these figures, the flexibility increasingfeatures 304 that constitute the region of increased flexibility 302 aremade in a “jigsaw” configuration that forms a sawtooth or zigzagpattern. Other possible features can have a pattern that is a“serpentine” configuration where the cuts are smoother, more rounded,and with a longer amplitude than the jigsaw pattern, for example butwithout limitation. Other types are possible and envisioned, includingstraight cuts, partial or dashed cuts, zigzag cuts, sinusoidal cuts, andso on. In some configurations, axially asymmetric cuts may be made so asto enhance flexibility in only one direction relative to the axis, forexample as discussed below in relation to FIG. 3F. Moreover, continuouspatterns are desired over interrupted patterns because of improvedresistance to fatigue failures and improved flexure characteristics.

FIG. 3C illustrates an embodiment of the region of increased flexibility302 comprising overlapping discontinuous straight reliefs 304, eachextending around approximately half of the circumference of the needlewall 300 in the illustrated configuration. In this embodiment, holes 306may be provided at one or more of the ends of each relief. The holes 306may in some cases be made as part of a laser cutting process used tocreate the reliefs 304, although the reliefs 304 and/or the holes 306may be made using any suitable process, for example chemical etching orwater jetting. The holes 306 may also be useful in providing additionalstrength to the needle wall 300, as it is believed that the holes 306may aid in reducing or eliminating the likelihood of crack propagationwhen the needle wall 300 undergoes various stresses.

FIG. 3D illustrates an embodiment with a region of increased flexibility302 comprising a single, continuous spiral cut 304. Holes 306, similarto those described above, may be present at the respective ends of thecut 304. Preferably, and as illustrated here, the pitch is substantiallyconstant throughout the length of the cut 304; in some embodiments,however, one or more portions of the cut 304 may have a varied pitch. Insome embodiments, a region of increased flexibility 302 may bemanufactured that resembles the embodiment illustrated here by using aclosely-spaced stacked wire, flat wire coil or cable tube. Of course,other embodiments may be manufactured using other types of cutting(e.g., laser cutting) discussed herein.

FIG. 3E is similar to the embodiment illustrated in FIG. 3C. Here,however, the region of increased flexibility 302 comprises aninterrupted spiral pattern where the tube has cut and uncut portionsalong the same spiral path 304 that have substantially the same pitchalong the entire length of the region 302.

FIG. 3F illustrates an embodiment with an asymmetric region of increasedflexibility 302. Here, cuts 304 can be positioned along only one side ofthe needle wall 300; in other words, the cuts 304 are arranged such thatonly a portion of the entire radial circumference along the axial lengthof the needle wall 300 is interrupted. In other words, when viewed alonga certain direction along the axial length of the needle wall 300, thecuts 304 forming a region of increased flexibility 302 will be seenalong at least a portion of one of the sides, while a side opposite thecuts 304 will be substantially lacking cuts. Arranged in this manner,the flexibility of the needle wall 300 along the region of increasedflexibility 302 will be asymmetrically flexible so as to permitincreased bending or flexibility in one direction or plane while beingless flexible in another direction.

Embodiments of needle walls 300 with asymmetrical regions of increasedflexibility may be useful in conjunction with bronchoscopes or othernavigational devices by increasing the maneuverability of the needlewall 300 while in the bronchoscope. In particular, some bronchoscopesmay be more adapted to bending in a particular plane—alignment of theasymmetrical region of increased flexibility 302 in this plane may thusbe useful. For example, asymmetric bending of the needle wall 300 canforce the needle wall 300 to rotate about its longitudinal axis as thenavigational device bends and flexes. Such rotation can help to ensurethat certain features of the needle could be maintained in asubstantially consistent alignment with regard to the navigationaldevice. For example, the bevel of the distal tip of the needle and/orultrasonic reflective zones of the needle walls 300 could be maintainedat a substantially consistent rotational orientation with respect thenavigational device (e.g., a bronchoscope). Further, rotation of theneedle wall 300 along its axial length may also aid navigation andmaneuverability, as certain embodiments with asymmetrical regions ofincreased flexibility 302 have been demonstrated to rotate in the pathof least resistance, typically the smallest possible radius.

The cuts 304 may not necessarily be straight and perpendicular to thelongitudinal axis of the needle wall 300. As illustrated in FIG. 3G, thecuts 304 that comprise the asymmetrical region of increased flexibility302 may be contoured, and may preferably further comprise a hole 306located in at least one of the ends 310 of one or more of the cuts 304.

Several characteristics of the cuts 304 may be altered to tailor thestiffness, bending resistance, torqueability, and other materialparameters of the region of increased flexibility 302. For example, thekerf, or cut width, in each cut 304 may be larger at some points than atothers, which may enhance flexibility. In some embodiments, the kerf ata midpoint 311 of a cut 304 may be wider than the kerf at one or more ofthe ends 310. In such a configuration, the flexibility may be increasedwhen the needle wall 300 is bent in the direction or plane of theasymmetrical region of increased flexibility 302, while reducing orminimizing flexibility (progressively or in a stepwise manner) as thebend location moves away from the direction or plane of the region ofincreased flexibility, as a result of the change in kerf toward the ends310. It may also be preferable to have a thinner kerf to reduce theamount of torque that can be applied to the needle wall 300 before thetube interlocks. Additionally, the kerf may be modified along the lengthof the region of increased flexibility 302. For example, the kerf in aproximal section may be wider and taper to a narrower kerf at the distalend, which may provide for a needle wall 300 that is flexible but thatwill stiffen when rotated.

Other characteristics of the region of increased flexibility 302 may bemodified. In addition to the kerf, the pitch spacing, the length and/oramount that a cut 304 extends around the needle wall 300, and thedistance between cuts 304 may be modified to tailor the wall 300 asdesired. In some embodiments, the minimum longitudinal distance pointbetween the cuts 304 can be varied along the length of the needle wall302. In some such embodiments, the flexibility of the needle wall 302can vary along the length of the needle (e.g., more flexibility as theminimal longitudinal distance between the cuts 304 is reduced).Accordingly, the flexibility, torqueability, and other characteristicsof the region of increased flexibility may be modified. Further, someembodiments may provide for a needle wall 300 comprising multipleasymmetrical regions of increased flexibility 302. In some embodiments,the multiple regions 302 may be staggered at differing orientations, forexample in mutually orthogonal directions (i.e., at 90° angles to eachother).

In practice, in tailoring the region of increased flexibility 302 andthe reliefs 304 that can constitute this region of increased flexibility302, it may be desirable to find a suitable balance between theflexibility required and the type of relief. For example, while wider orlarger reliefs may provide additional flexibility, these may in somecases weaken the needle wall 300 to an unacceptable extent. Differentpatterns also may perform more or less satisfactorily in fatiguetesting. Additionally, certain patterns may cause portions of the regionof increased flexibility 302 to abrade the working channel of thecatheter or other instrument the needle is inserted in, or else thetissue being biopsied (although this may be desirable in certainapplications, as described below). Postprocessing after creation of thereliefs may include steps such as deburring, electropolishing, extrudehoning, microblasting, or ultrasonic cleaning, which may at leastpartially alleviate or reduce such concerns. The type of reliefs 304described above may also be adjusted in accordance with the length ofthe one or more regions of increased flexibility 302. Prototypes havebeen constructed with regions of increased flexibility measuringapproximately 3-4 cm. Preferably, the extreme distal end of the needlewall 300 is left uncut or otherwise generally solid to reduce thelikelihood of buckling and so that a piercing point can be made onto theneedle. In some arrangements, the piercing point is ground or honed andthe generally solid portion of the extreme distal end assists in theformation of a point or tip. In some embodiments, the generally soliddistal region measures between about 8 mm and about 10 mm. Otherconfigurations are possible.

FIG. 4 shows an embodiment of a flexible transbronchial needle 400 thatcomprises a distal tip portion 402 and a flexible region 404. In oneembodiment, the distal tip portion 402 has a sharply angled tip to coreor scrape cells from tissue to be sampled. The flexible region 404preferably comprises one or more reliefs or cuts 406. In one embodiment,the cuts 406 are a jigsaw cut. In other embodiments, the cuts 406 may bea different type of cut, for example as described above in FIGS. 3A-G.In one embodiment, a covering 408, which may comprise polymer coatingsand/or heat shrink wrap, can be used to cover the cuts 406 on the needle400. The covering 408 may in some embodiments also comprise coils of aresilient material (e.g., metals or polymers) that surround at least aportion of the flexible region 404 to provide additional support againstbuckling or collapse, while remaining flexible enough to provideselective articulation and/or bending of the needle 400.

Obtaining a cored tissue sample may be preferable for pathology orhistology samples where a largely-intact sample of tissue is desired.For such applications, the needle is preferably in a relatively largersize range of approximately 17-19 gauge, possibly with a smaller 21gauge needle within. Such needle sizes have been found to produce a“cored” tissue sample satisfactory for histology applications. Obtainingbiopsy cells and fluid for cytology may however use a smaller, non- orminimally-coring distal tip portion 402, for example. Because biopsiesfor cytological applications typically apply suction while performingagitation (moving back and forth) of the needle in the biopsy site,sharper and/or rougher needles may perform better and obtain additionalcells. For such applications, smaller needle sizes in the range of 21-23gauge may also be preferable. In some embodiments, the distal tipportion 402 may be cut and/or angled differently for differentapplications. In some applications, a hole, port, slot or otherstructure also can be provided just proximal of the distal end. In someapplications, the hole, port, slot or other structure can be provided ona surface of the needle that is opposite from the surface of the needlehaving the most proximal portion of the beveled opening formed at thetip. In some applications, the hole, port, slot or other structure ispositioned within a region defined between the distal tip and the mostproximal portion of the opening formed by the beveled surface of theopening at the tip. A vacuum source may also be provided so as toaspirate a tissue sample or samples. Other configurations also arepossible.

The cuts 406 on the flexible region 404 may be suitable for cytologicalbiopsy procedures. Here, a cut may provide rougher edges that can scrapecells along the path of the needle 400. For example, when theinterrupted surface of the needle is bent, the cuts can create ascalloped surface. In particular, sinusoidal, “jigsaw,” “serpentine,” orzigzag cuts may provide for rougher edges, which—especially when theneedle 400 is bent or articulated—can abrade the surrounding tissue andthus sample additional cells. These abraded cells can then be aspiratedvia the needle 400 along with any other sample being biopsied. If nocoating and/or heat shrink wrap 408 is present over the cuts 406, theresulting small openings may also be used to aspirate the abraded cellsinto the needle 400. Such an uncoated portion of the cut section 406, ifpresent, is preferably located at the distal end of the needle 400 suchthat surrounding tissue may ingress into the inner lumen during suction.

To increase this scraping or scalloping effect, several steps may betaken. If the cuts 406 are made by water jetting, the needle 400 may beextrude honed to push burrs outward, increasing the roughness of theflexible region 404. Likewise, laser cutting the cuts 406 may in somecases provide additional roughness. In some cases, a polishing ordeburring step may be necessary. Dimpling or grinding of the cuts 406and/or the region 404 may also be useful. The kerf (or width) of thecuts 406 may also be increased, either in part or in whole, along theflexible region 404, which may consequently enhance the scraping orscalloping effect.

The needle 400 may also be flushed after being withdrawn no as to obtainany remaining cells. In some cases, the operator using a needle 400 withcuts 406 will preferably navigate the needle 400 so as to reduce thelikelihood of abrading or puncturing blood vessels in the biopsy region,because the resulting jagged edges may take longer to stop bleeding thana cut resulting from a biopsy needle lacking cuts. In someconfigurations, a dual-needle configuration, with a relatively smoothneedle used to puncture into the biopsy site, followed by largerdiameter, flexible needle that can include scalloped surfaces that canbe used to scrape the tissue. Quick-clotting or cauterizing featurescould also be incorporated into the needle 400 or various other systemcomponents to minimize bleeding when piercing tissue.

FIG. 5 illustrates an embodiment of a flexible transbronchial needle500. The needle 500 comprises several interconnected portions. Aproximal end of the needle 500 comprises a less flexible shaft portion502. A distal end of the needle 500 comprises a more flexible shaftportion 504. The less flexible shaft portion 502 and the more flexibleshaft portion 504 can be connected together by the tapered shaft section524 in the illustrated configuration. In some configurations, however,the less flexible shaft portion 502 and the more flexible shaft portion504 can be integrally formed. The more flexible shaft portion 504comprises a distal tip portion 508 and a cut section 510. Cuts 512 arelocated within the cut section 510. The cuts can be formed in anysuitable manner. In one embodiment, the cuts 512 are a “jigsaw” cut, asdescribed above with reference to FIGS. 3A-C. In other embodiments, thecuts 512 may be cut differently.

This embodiment of a flexible transbronchial needle 500 has severaladvantages, as on one hand the needle 500 becomes more torquable andpushable while also retaining flexibility at its distal end. The lessflexible shaft portion 502 at the proximal end is preferably more rigidand stiffer than the more flexible shaft portion 504, so as tofacilitate torque and force transmission to the thinner, more flexibleshaft portion 504. In one embodiment, this is accomplished byconstructing the needle 500 so as to become progressively thinner fromthe proximal end to the distal end, such that the flexible shaft portion504 remains flexible and bendable. By constructing the needle 500 in amanner that it becomes thinner at the tapered shaft portion 524, theneedle becomes more flexible, while also reducing resistance to rotationin the distal end comprising the flexible shaft portion 504.Additionally, the more rigid portion 502 is more durable and better ableto transmit torque or force, while being situated in a portion of theneedle 500 where flexibility is less important.

The less flexible shaft portion 502 has an outside diameter D1 514. Themore flexible shaft portion 504 has an outside diameter D2 516. Thetapered shaft section 524 has a proximal end 518 and a distal end 520,with the outside diameter D3 522 being located at the proximal end ofthe tapered shaft section 518 and the outside diameter D4 520 beinglocated at the distal end of the tapered shaft section 520. Preferably,the outside diameter D3 522 is equal to the outside diameter D1 514. Theoutside diameter D4 520 is preferably equal to the outside diameter D2516. The outside diameter of the tapered section 524 may vary linearlyor nonlinearly between D3 and D4. It will also be understood that insome embodiments, the tapered section 524 may extend into all or part ofthe flexible shaft portion 504 and/or the less flexible shaft portion502, and that in some embodiments there may be additional taperedsections. Further, although the tapered section 524 reduces in diametergoing in a proximal to distal direction, the opposite configuration maybe useful in some embodiments.

Typically, the portions 502, 524, 504 will be constructed from a lengthof material (e.g., metals such as stainless steel or nitinol) of asubstantially uniform thickness, and as such, the inside diameters ofthe respective portions will generally correlate to the outsidediameters referred to above. However, it is contemplated that materialsof varying thicknesses may be used to construct the needle, and thethickness defined by the inside and outside diameters may differ alongthe length of the device. This may be accomplished, for example, byconstructing the needle 500 in a piecewise fashion from separate parts,or by drawing out the needle in a single unit so as to create sectionsof varying thickness. Such varying thicknesses may be used, for example,to tailor factors such as the rigidity, strength, torquability, orflexibility of the resulting needle to the desired application.

FIGS. 6A-D illustrate different embodiments of steerable, flexibletransbronchial needle aspiration assemblies. Such assemblies may bemanipulated by an operator to steer the needle to a site identified tobe of interest. Preferably, such assemblies may also permit a flexibleneedle to be steered independently of a bronchoscope or other endoscope.While the examples discussed below in FIGS. 6A-D discuss a needleaspiration assembly, in some embodiments, a guide sheath provided withthe steerable features discussed below may also be used. In such anembodiment, a needle, preferably a flexible needle, may be insertablethere through.

In FIG. 6A, a flexible transbronchial needle aspiration assembly 600Acomprises a flexible transbronchial needle 602A and a steering wire604A. In FIG. 6B, a flexible transbronchial needle aspiration assembly600B comprises a flexible transbronchial needle 602B, a first steeringwire 604B and a second steering wire 606B. In FIG. 6C, a flexibletransbronchial needle aspiration assembly 600C comprises a flexibletransbronchial needle 602C, a first steering wire 604C, a secondsteering wire 606C and a third steering wire 608C. In FIG. 6D, aflexible transbronchial needle aspiration assembly 600D comprises aflexible transbronchial needle 602D, a first steering wire 604D, asecond steering wire 606D, a third steering wire 608D and a fourthsteering wire 610D. These steering wires can be arranged in differentmanners to achieve different steering characteristics. Certainembodiments provide for the steering wires to angle or bend the needle602 at an angle of up to 45 degrees. Certain embodiments may be smallenough to fit within a 2.0 mm working channel of a bronchoscope, and maybe miniaturized further.

In these preceding figures, the steering wires may be manipulated by theoperator to guide a flexible transbronchial needle to a site ofinterest. Preferably, this is accomplished by using the one or moresteering wires to pull (and thereby bend) the flexible needle in thedirection desired. The wires may be attached to the flexible needle inany suitable manner, on the interior or exterior of the flexible needle.In some configurations, the wires are secured by welding them to theflexible needle. When wires are attached to the interior of the flexibleneedle, such embodiments may allow for insertion into a smaller sheathor working channel. In certain embodiments, this may be accomplished byhaving the steering wire comprise one or more pull wires. Bowden cablesmay be used in some embodiments. Nitinol wires, which contract afterbeing heated past a transition temperature may also be used, possibly inconjunction with a heating element controllable by the operator (forexample, by using resistive heating).

FIG. 7 shows an embodiment of a steerable, flexible transbronchialneedle aspiration assembly 700. The needle 700 comprises a flexibleshaft portion 702 at the distal end. The flexible shaft portion 702comprises a distal tip portion 704 and a flexible section 706 that maybe selectively elastically bent or angled such that the respective endsare no longer collinear. The flexible section 706 comprises cuts 707that may be covered and/or sealed with a coating 709, for example apolymer and/or heat shrink. The cuts 707 may be of the type previouslydescribed, and could be, for example, “jigsaw” cuts.

In some embodiments, a steering wire 708 is located along the exteriorof the flexible shaft portion 702. In other embodiments, multiplesteering wires 708 are located along the exterior of the flexible shaftportion 702; these may be arranged as depicted above in FIGS. 6A-D. Thesteering wire or wires 708 may, as described in FIGS. 6A-D, be used toguide the needle 700 to the site to be biopsied. Preferably, a seal 710covers at least a portion of the exterior of the steering wires 708 andthe flexible shaft portion 702 to reduce the likelihood of the steeringwires snagging equipment or body tissue, and preferably is constructedfrom a pliable polymer.

The proximal end of the needle 700 may be part of or joined to a steelhypotube 711. The proximal end of the hypotube 711 may also have aconnection 714 (for example, a luer fitting) so that a source of vacuum(for example, a pump or syringe 712) can be used to pull a vacuum alongthe length of the hypotube 711. In a preferred embodiment, the hypotube711 is manufactured from any suitable material.

FIG. 8 illustrates an embodiment of a flexible steerable needle 800comprising an inner guidewire 810. Here, the inner guidewire 810 can bepositioned along a central lumen of an embodiment of a flexible needle800, which may be designed in a similar manner as other embodimentsdescribed herein. In some configurations, the guidewire 810 has a lengththat is greater than the length of the needle 800.

The needle 800 preferably comprises a distal tip portion 802 with adistal opening 803. A flexible section 804 preferably is configured tobe more flexible than the distal tip portion, and may comprise cuts 806of the type previously described. These cuts 806 confer additionalflexibility to the needle 800 and permit it to bend or curve. In someembodiments, all or part of the flexible section 804 (and the cuts 806)may be covered with a coating 808, which may be a polymer and/or heatshrink, for example but without limitation.

The guidewire 810 preferably is constructed from a shape memory material(metal or polymer) such as Nitinol. Preferably, the guidewire 810 is setin a form that will curve when heated, but is inserted into the needle800 while in a straightened configuration. While the guidewire 810 isinserted into the needle 800, heating of the guidewire 810 will cause itto curve, thereby curving the needle 800 along its flexible section 804.In some configurations, the guidewire 810 simply is inelasticallydeformed to provide nonlinear region proximate the distal end. In suchconfigurations, simply inserting the guidewire 810 into the needle 800can cause the needle to bend.

In use, the curved guidewire 810 can be used to steer the needle 810 byrotating the guidewire 810 relative to the needle 810. The curve or bendin the guidewire 810 will cause the flexible portion of the needle 810to deflect such that the direction of the needle 810 can be varied. Insome embodiments, rotational alignment of the curved guide wire 810 withrespect to the needle 800 can be controlled using an asymmetricdistribution of cuts on the needle wall (e.g., as described above withregard to FIGS. 3F and 3G). For example, asymmetric cuts on the needlewall can cause the needle 800 to rotate about its longitudinal axis asthe needle 800 bends to conform to the bent shape of the guidewire 810.In some embodiments, asymmetric cuts in the needle wall help to ensurethat the guidewire 810 remains aligned in the same plane of the needle800 as the bent portion of the guidewire 810 passes through the flexiblesection 804 of the wire 800. The guidewire 810 may also be used tonavigate the needle 800 to the site of interest. Here, the guidewire 810is guided to the region of interest (e.g., a lung nodule), and theneedle 810 is then pushed along the guidewire 810 until the region ofinterest has been reached. The guidewire 810 may then be withdrawn so asto permit aspiration and biopsying of the region of interest. Partlybecause the guidewire 810 is located inside the needle 800 and thusprovides a very small diameter probe, such a system may be employed tonavigate to peripheral lung regions of a reduced diameter and that areinaccessible with a bronchoscope. Additionally, because the guidewire810 is positioned inside of the needle 800, such a configuration may bepreferable for biopsying samples via scraping or scalloping of tissuewith the flexible section 804. When the guidewire 810, or anothercomponent associated with one or more of the guidewire 810 and theneedle 800, is radioopaque, fluoroscopy or the like may be used tonavigate the guidewire to a region of interest. Typically, the needle800 and guidewire 810 are contained within a catheter or sheath. Uponreaching an airway wall proximate to a region of interest, either theneedle 800 or the guidewire 810 can be extended into a nodule or othertissue at the region of interest. In some configurations, the needle 800may extend between 15-20 mm into the adjacent tissue from the end of thecatheter or sheath. In some embodiments, the needle 800 may beconfigured to extend up to about 40 mm into adjacent tissue.

In certain embodiments, the curved guidewire 810 may be part of a systemused for providing repeatable access and/or navigation to regions of thelung. Such embodiments are described in Provisional Application Ser. No.61/604,462, filed Feb. 28, 2012, titled “PULMONARY NODULE ACCESS DEVICESAND METHODS OF USING THE SAME”, and the application is herebyincorporated by reference in its entirety. Such embodiments are alsodescribed in U.S. patent application Ser. No. 13/778,008 (AttorneyDocket No. SPIRTN.082A), filed Feb. 26, 2013, titled “PULMONARY NODULEACCESS DEVICES AND METHODS OF USING THE SAME” and published as U.S.Patent Publication No. US 2013-0226026 A1, and the publication is herebyincorporated by reference in its entirety.

FIG. 9 illustrates an embodiment similar to that illustrated in FIG. 8.Here, a connector 814 is connected to the proximal end of the hypotubeof the needle 800. The connector 814 used here can be any type ofsuitable connector, including for example a luer connector. Theguidewire 810 is introduced through the connector 814, and at theproximal end of the guidewire 810 is a handle 816 that permits theguidewire 810 to be pushed, pulled, and rotated with respect to theneedle 800. After the guidewire 810 has used to guide the needle 800 tothe biopsy site, the guidewire 810 is removed from the connector 814. Asource of vacuum (e.g., a syringe) is then attached to the connector 814to aspirate the biopsy sample from the needle 800.

FIG. 10 is an annotated fluoroscopy image of a curved guidewire similarto that described in FIG. 8 being used to biopsy a lung nodule. Here,the catheter 1000 extends from the distal end of a bronchoscope 1014.The lung passages here were too small to permit navigation of thebronchoscope to an area near the lung nodule, and as such, the catheter1000 was advanced via fluoroscopy to the suspected nodule site 1012. Thedistal end of the lumen 1002 containing the flexible needle 1006 alsocontains coils 1004, which reinforces the lumen 1002 while the needle islocated within the lumen and also serves as a fiducial radioopaquemarker helpful for visualization of the catheter 1000 in relation to thenodule site 1012. Additional fiducials may also be added to variouscomponents of the catheter 1000 (e.g., barium sulfate markers).Extending distally to the needle 1006 is a guidewire 1008, which, beingcurved, aids in guiding the flexible needle 1006 to the nodule site1012. In use, the flexible needle 1006 is pushed over the guidewire 1008to the nodule 1012, the guidewire 1008 is withdrawn and biopsy tissuesamples are aspirated through the flexible needle 1006.

A method of obtaining a tissue sample may comprise advancing thebronchoscope 1014 toward a tissue site (e.g., a lung nodule 1012 orlymph node). Within the bronchoscope 1014, the catheter 1000 may bemovably disposed. In some embodiments, and preferably when advancing totissue regions in small or convoluted airways that may not permitnavigation with the bronchoscope 1014, a guide sheath surrounding thecatheter 1000 may be advanced beyond the bronchoscope 1014 instead of orin conjunction with the guidewire 1008. In some embodiments, the guidesheath may be used without the bronchoscope 1014. The guide sheath maybe used in conjunction with a location device, such as fiducial markers(e.g., coils 1004) or an ultrasound probe (e.g., as described below inFIGS. 11A-C). Preferably, the location device is present on the catheter1000, although a location device may be instead or also present on theguide sheath. Once proximate the tissue site, the catheter 1000 may beadvanced beyond the guide sheath and navigated to the tissue site (e.g.,using the location device placed thereon) so as to obtain a sample withthe flexible needle 1006. The entire assembly may then be withdrawn, orcertain portions thereof (e.g., coils 1004) may be implanted proximatethe tissue site to serve as a marker.

FIG. 11A shows a cross section view of an embodiment of a multi-lumen,steerable catheter 1100 which may be configured for introduction into abodily space (for example, pulmonary passages) via an endoscope such asa bronchoscope. The catheter 1100 preferably comprises a first lumen1102 and a second lumen 1104, although other embodiments may comprise acatheter 1100 with more than two lumens. The first lumen 1102 may belarger than the second lumen 1104. In a preferred embodiment, the firstlumen 1102 may be used to introduce a miniaturized ultrasound probe,which may then be used to provide real-time location information of thebodily tissues to be examined. For example, when used in the lungs anultrasound probe can be useful to locate nodules or other locations(e.g., lymph nodes) of suspected or actual cancerous tissue which may bedifficult or impossible to locate visually. Preferably, the second lumen1104 is used to introduce various tools, including but not limited totransbronchial aspiration needles, cytology brushes, biopsy forceps,guiding devices, and so forth.

The catheter 1100 also preferably comprises at least one steering wire1106, which preferably is connected to the second lumen 1104 to permitselective articulation and bending of the distal end of the second lumen1104. The steering wire 1100 is preferably of the type that may be usedin the embodiments described above in FIGS. 11A-D. It is to be notedthat whereas the embodiments illustrated in FIG. 8 have an innerguidewire 810 introduced within the inner diameter of the needle 800,the embodiments illustrated in FIGS. 11A-C disclose steering wirespositioned on the outside of the needle. This is not to say that the twoapproaches are mutually incompatible—embodiments may be designed usingboth inner and outer steering.

FIGS. 11B and C illustrate side views of an embodiment of a multi-lumen,steerable catheter 1100. This catheter 1100 comprises a first lumen 1102and a second lumen 1104. The second lumen 1104 comprises a steering wire1106. FIG. 11B illustrates the second lumen 1104 in a relaxed,non-articulated state.

FIG. 11C shows a side view of an embodiment of a multi-lumen, steerablecatheter 1100 used to visualize and conduct a biopsy on a target nodule1112 located behind an airway wall 1110. Here, the catheter 1100 isillustrated with an ultrasound probe 1116 inserted into the first lumen1102. The ultrasound probe 1116 is preferably a miniaturized ultrasoundprobe configured to be inserted into a small catheter or endoscope, andcan be for example the UM-S20-17S radial endoscopic ultrasound probemanufactured by Olympus. Such miniaturized ultrasound probes may beadvantageous for localization and visualization in peripheral lungpassages where visual observation (i.e., via a bronchoscope) isextremely difficult due to the small size of such passages. The secondlumen 1104 is illustrated with a flexible needle 1114 insertedtherethrough and preferably moveable in a longitudinal back and forthdirection so as to biopsy the target nodule 1112. In the illustration,the steering wire 1106 is pulled, thus selectively articulating thesecond lumen 1104 at an angle with respect to the first lumen 1102. In apreferred embodiment, the needle 1114, when fully extended, canarticulate or bend at an angle of about 40 degrees with respect to thefirst lumen 1102. In some embodiments, the steering wire 1106 may angleor articulate both lumens 1102 and 1104. Some embodiments may alsoprovide for multiple steering wires 1106 capable of both lumens 1102 and1104 independently. In further embodiments, the steering wires may beprovided directly onto the flexible needle 1114 and/or ultrasound probe1116.

Articulating the distal end of the second lumen 1104 of the catheter1100 allows tools, in this case distal end of the needle 1114, to beangled toward the target nodule 1112 while the ultrasound probe 1116remains in the airway providing real-time location confirmation that theneedle 1114 has reached the target nodule 1112. Accordingly, the angleof the second lumen 604 preferably is adjusted and aligned such that theneedle 1114 and nodule 1112 simultaneously remain in the field of view1118 of the ultrasound probe 1116. Embodiments of the catheter 1100 havebeen constructed wherein the needle 1114 is able to articulate up to 20degrees relative to the ultrasound probe. Some embodiments have beenconstructed that are compatible with a 3.2 mm bronchoscope workingchannel, and may be miniaturized further.

FIGS. 12A-C illustrate a bronchoscope in various degrees ofarticulation. FIG. 12A illustrates the articulation of a bronchoscopewithout any biopsy needle inserted within. Here, the angle ofarticulation is approximately 130 degrees. FIG. 12B illustrates thearticulation achievable by the same bronchoscope with a conventionalstraight rigid biopsy needle and catheter inserted therein. Thearticulation angle here is only about 90 degrees. Finally, FIG. 12Cshows the same bronchoscope with an embodiment of a flexible needleinserted therein. The needle may for example be of the type illustratedin FIG. 2. Due to the flexibility of the needle, the articulation angleachieved here is approximately 130 degrees, and the bronchoscope'soverall flexibility is minimally altered in comparison to thebronchoscope without any needle inserted.

FIGS. 13A-C illustrate an embodiment of a flexible needle with steeringwires similar to those illustrated in FIGS. 6A-D and FIG. 7. FIGS. 13A-Bshow that the needle, with the steering wire pulled, can achieve anarticulation of approximately 45 degrees. FIG. 13C illustrates a closeupof the distal end of the needle. A polymeric covering coats or coversthe distal end just short of the distal tip of the needle and covers thesteering wire or wires underneath.

FIGS. 14A-B illustrate an embodiment of a flexible needle 1002 insertedinto a multi-lumen, steerable catheter 1000 similar to FIG. 11C. Theprobe 1006 may be a miniaturized ultrasound probe, and is preferablyinserted into one of the catheter lumens. In FIG. 14A, the flexibleneedle 1002 is shown in a retracted configuration and is inside a sheath1004. FIG. 14B shows the flexible needle 1002 in an extended positionand articulated. The needle 1002 may be articulated, for example, usingthe steering wires described above in relation to the embodiment in FIG.11C. Here, the needle can achieve an articulation of approximately 20degrees relative to the distal end of the probe 1006.

FIGS. 15A-C illustrate various states of articulation of a bronchoscopecomprising an ultrasound probe similar to that illustrated in FIG. 1.First, FIG. 15A shows the articulation of the bronchoscope without anybiopsy needle inserted therein. The bronchoscope can achieve anarticulation of approximately 110 degrees. FIG. 15B shows thebronchoscope with a conventional straight biopsy needle and catheterinserted therein. The bronchoscope's articulation is reduced toapproximately 50 degrees, with the straight needle providingapproximately 20 degrees of additional angle (for a total of 70degrees). FIG. 15C shows the same bronchoscope with a flexible needleand catheter inserted therein similar to the embodiment illustrated inFIG. 2. Here, the bronchoscope can bend to approximately 90 degrees,with the flexible needle providing approximately additional 20 degreesof additional angle (for a total of 110 degrees). It is important tonote that the flexible needle illustrated in FIG. 15C is not beingarticulated independently of the bronchoscope, and an additionalindependent articulation mechanism (including for example but withoutlimitation the embodiments illustrated in FIGS. 6A-D and/or FIG. 8) canprovide for additional angulation and articulation of the needle topermit access to tortuous spaces.

FIGS. 16A-C illustrate another embodiment of a flexible needle andcatheter, of which the needle may be similar to the embodimentillustrated in FIG. 2. FIGS. 16A-B depict the articulation of the needleindependent of any steering mechanism, and show that the needle can bendapproximately 90 degrees. FIG. 16C is a close up of the flexible needle1002, and illustrates a needle sheath or catheter 1004 covering the moreproximal section of the flexible needle 1002. The flexible needle 1002extends past the distal end of the sheath 1004, and has a flexiblesection 1008 (similar to the flexible shaft portion 204 discussed above)that comprises spiral “jigsaw” cuts covered with a layer of heat shrinkmaterial. The extreme distal tip 1010 of the flexible needle isuncovered and lacks cuts, and is sharpened so as to pierce into tissue.

FIG. 17 illustrates a handle 1701 that may be used to manipulate andcontrol embodiments of the flexible needles described herein. The handle1701 is connected to a catheter 1700 with a flexible needle hypotubewithin, and the handle 1701 can control the extension of the needle fromthe catheter.

FIG. 18 is a closeup view of an embodiment of a flexible needle 1802.This embodiment has a flexible section 1804 comprising a spiral cut1806, and which extends close to the extreme distal tip 1810 of theflexible needle 1802. The distal tip 1810 is preferably beveled andsharpened so as to penetrate into tissue. The proximal end 1809 of theflexible needle may be optionally covered by a polymeric sheath 1812with coils 1814 underneath and overlying the body of the flexible needle1802. Preferably, the coils 1814 provide structural support to theneedle 1802 to reduce or eliminate the likelihood that the needle 1802will prolapse or collapse, in particular when the needle 1802 is bent orarticulated.

FIG. 19 is a fluoroscopy image similar to that illustrated in FIG. 10.Here, a bronchoscope of the right side of the image has a catheterextending from it. The catheter comprises a coil at its distal end thatmay aid visualization of the device. A flexible needle also extends fromthe distal end of the catheter and is depicted here piercing into andbiopsying a lung nodule (the darker circular object on the left). Theflexible needle is guided by an inner guidewire similar to theembodiment illustrated in FIG. 8.

It will be understood that the present descriptions of the lung biopsysystems, apparatuses, and methods described herein as being used in alung and for lung nodules are not limiting, and that these embodimentsmay be used for biopsying, navigating, and locating areas of interest inother locations on a patient, including gastric, endoscopic, or othersuitable locations. Similarly, a bronchoscope is not necessary, andother suitable devices capable of accommodating the embodimentsdescribed herein may also be used, including without limitation variousendoscopes or laparoscopic cannulas.

As illustrated in FIG. 20A, a substance delivery system 2000 can includea delivery needle 2010. In some embodiments, the delivery needle 2010can be similar to or the same as the flexible TBNA needles describedherein. The delivery needle 2010 can be hollow. In some embodiments, thedelivery needle 2010 defines a delivery lumen 2012 and has a deliveryneedle wall 2019. The delivery needle wall has an internal surface 2021and an outside surface 2022. The delivery lumen 2012 can extend throughthe distal end 2014 of the delivery needle 2010. In some embodiments,the delivery lumen 2012 extends through the entire length of thedelivery needle 2010. The delivery needle 2010 can include a solid(e.g., without an internal lumen) portion (not shown) at and/or near aproximal end of the delivery needle 2010. In some embodiments, thedistal end 2014 of the delivery needle 2010 can be configured to piercetissue within the body. For example, the delivery needle 2010 can bebeveled or otherwise sharpened at its distal end 2014. The deliveryneedle 2010 can be navigated to a site of interest (e.g., a nodule,lesion, or other site of interest) within the body via the workingchannel of a delivery device (e.g., a bronchoscope, endoscope). In someembodiments, the delivery needle 2010 is navigated to the site ofinterest using a catheter. The delivery needle 2010 can be positionedwithin a sheath to protect the distal end 2014 and/or the workingchannel of the delivery device or catheter from damage. The sheath canbe retracted from the delivery needle 2010 prior to deploying the needle2010 to the site of interest. In some embodiments, the delivery needle2010 can be advanced distally past the distal end of the sheath in amanner similar to the needles described above.

In some embodiments, at least a portion of the length of the deliveryneedle 2010 is flexible. For example, delivery needle 2010 can includeflexibility increasing features similar to or the same as thosedescribed with respect to the flexible and/or transbronchial needlesabove. Such flexibility increasing features can include cuts in the wall2011 of the delivery needle 2010. In some embodiments, one or more cutpatterns can be cut into portions of the wall 2011 of the deliveryneedle 2010. For example, jigsaw cuts, straight cuts, spiral cuts,interrupted spiral cuts, partial or dashed cuts, zigzag cuts, sinusoidalcuts, and/or any combination of these or similar cuts would be made in aportion of or along the entire length of the wall 2011 of the deliveryneedle 2010.

According to some variants, the wall 2011 of the delivery needle 2010 iscoated. For example, the interior surface and/or exterior surface of thewall 2011 can include a heat shrink material or some other coating. Thecoating can be configured to reduce or eliminate the likelihood thatfluid would leak through the wall 2011 between the delivery lumen 2012and the surroundings of the lumen 2012.

As illustrated in FIGS. 20A-20B, one or more internal flexible needles2040 can be positioned within the delivery needle 2010. For example, theinternal flexible needles 2040 can be sized (e.g., have diameters) suchthat three internal needles 2040 can be stored within the deliveryneedle 2010. Many variations in the number of needles 2040 configured tofit within the delivery needle 2010 are possible (e.g., 2 needles, 4needles, 6 needles).

In some embodiments, the internal needles 2040 extend the length of thedelivery needle 2010 (e.g., from the proximal end of the delivery needle2010 to the distal end 2014 of the delivery needle 2010). Preferably,the internal needles 2040 can be attached to a flexible shaft 2030. Theflexible shaft 2030 can comprise a tube comprise a polymer tube, ametallic or polymer coil, and/or a laser or chemical cut hypotube. Insome embodiments, the internal needles 2040 are attached to the distalend of the flexible shaft 2030 via a collar 2020. The collar 2020 canbe, for example, an adhesive binding. In some embodiments, the collar2020 can be constructed from a metallic material onto which the interiorneedles 2040 can be welded or otherwise adhered. In some embodiments,the internal needles 2040 are coupled with the flexible shaft 2030directly, without the use of a collar 2020.

As illustrated in FIG. 20B, the internal needles 2040 can be hollow andcan define internal needle lumens 2048. The internal needle lumens 2048can be in fluid communication with an interior lumen of the flexibleshaft 2030. In some embodiments, the proximal ends of the flexible shaft2030, the internal lumen 2012, and/or internal needle lumens 2048 are influid communication with a delivery fluid source. For example, theinternal needle lumens 2048 can be in fluid communication with anexternal fluid source (e.g., a syringe, a peristaltic pump), eitherdirectly or via the interior lumen of the flexible shaft 2030.

The flexible shaft 2030 and/or internal needles 2040 can be configuredto move in the distal and/or proximal directions with respect to thedelivery needle 2010. For example, the internal needles 2040 can beconnected to a proximal handle (not shown), either directly or via theflexible shaft 2030. The proximal handle can be configured to move theflexible shaft 2030 and/or internal needles 2040 in the proximal anddistal directions with respect to the delivery needle 2010. In someembodiments, a first proximal handle can be connected to the flexibleshaft 2030 and a second proximal handle can be connected to the internalneedles 2040. In some embodiments, the internal needles 2040 can bemoved in the proximal and distal directions with respect to the flexibleshaft 2030 and/or the collar 2020. In some embodiments, each of theinternal needles 2040 can be individually (or, e.g., in subsets of thewhole set of internal needles 2040) connected to a proximal handle. Insome such embodiments, each (e.g., or each subset) of the internalneedles 2040 can be moved in the distal and proximal directions withrespect to the other internal needles 2040.

The internal needles 2040 can be constructed from a metal or metalalloy, such as stainless steel, steel, titanium, or some otherappropriate material. In some embodiments, the internal needles 2040, orsome portion thereof, are constructed from a polymer or othernon-metallic material. Preferably, at least a portion of each of theinternal needles 2040 is constructed from nitinol or some othershape-memory material.

In some embodiments, the internal needles 2040 are configured totransition between a contracted position (e.g., as illustrated in FIGS.20A-20B) and an expanded position (e.g., as illustrated in FIGS.21A-21B). In the expanded position, the internal needles 2040 can flareout from the distal end 2014 of the delivery needle 2010. In someembodiments, the internal needles 2040 transition from the contractedposition to the expanded position as the distal ends 2046 of theinternal needles 2040 pass the distal end 2014 of the delivery needle2010. In some embodiments, the wall 2011 of the delivery needle 2010includes one or more apertures through which the internal needles 2040can pass when transitioning between the contracted position and theexpanded position. The extent to which the internal needles 2040 flareout from the distal end 2014 of the delivery needle 2010 can, in someembodiments, be controlled by the relative distal movement of theinternal needles 2040 relative to the delivery needle 2010. For example,once past the distal end 2014 of the delivery needle 3010 (or, e.g.,through the apertures in the wall 2011 of the delivery needle 2010), thedistal ends 2046 of the internal needles 2040 can be configured to flareout further from the delivery needle 2010 as the flexible shaft 2030and/or internal needles 2040 are advanced in the distal directionrelative to the delivery needle 2010. The interior surface of the wall2011 of the delivery needle 2010 can include a coating to reduce oreliminate the likelihood that the internal needles 2040 would catch onthe interior surface of the wall 2011 as the internal needles 2040translate in the proximal and/or distal directions with respect to thedelivery needle 2010.

The internal needle lumen 2039, having walls 2041, of the internalneedles 2040 can include cut (e.g., laser cut and/or chemical cut)features 2042 such as, for example, holes or slits. The cut features2042 can facilitate fluid communication between the internal needlelumens 2048 and the tissue into which the internal needles 2040 aredeployed. The cut features 2042 can be placed on the sides of theinternal needles 2040 that are compressed and stretched as the needles2040 deploy from the distal end 2014 of the delivery needle 2010 In someembodiments, the cut features 2042 are made into the sides of theneedles 2040 tangential to the direction of bending as the needles 2040extend from the distal end 2014 of the delivery needle 2010 (e.g., asillustrated in FIG. 21A). According to some variants, the cut features2042 are located at various points around the wall of the needles 2040.In some embodiments, the distal ends 2046 of the internal needles 2040include distal apertures 2044 at a distal end 2045 in fluidcommunication with the internal needle lumens 2048 of the internalneedles 2040.

The internal needles 2040 and/or delivery needle 2010 can be configured(via, e.g., cut features and/or cut patterns in the walls 2041, 2011 ofthe needles 2040, 2010) to be flexible such that the delivery needle2010 can be navigated to and/or through narrow and/or tortuous lumenswithin the body. As such, the substance delivery system 2000 can bedelivered to a site of interest within the body using the body's naturalorifices (e.g., the mouth). In some embodiments, piercing of tissuewithin the body (other than piercing an airway wall to access extrinsicareas of interest outside of the airway) can be avoided by using aflexible substance delivery system 2000 as described. According to somevariants, the delivery needle 2010 and internal needles 2040 can benavigated to the site of interest (e.g., nodule, tumor, lesion) to betreated using a bronchoscope of other delivery device. For example, thedelivery needle 2010 can be delivered to a site of interest in the lungvia a bronchoscope inserted through the airways of the throat and lung.In some embodiments, the delivery needle 2010 is navigated to the siteof interest thoracoscopically (e.g., through an incision in torso of thepatient). In some embodiments, the delivery needle 2010 can be navigatedto the site of interest using a delivery catheter similar to or the sameas the delivery catheter 1100 described above with respect to FIG. 11C.For example, an ultrasound probe 1116 can be used to navigate thedelivery needle 2010 to the site of the interest. The ultrasound probe1116 can facilitate real-time tracking of the needle 2010 as the needle2010 is navigated to the site of interest.

FIG. 22A illustrates an embodiment of a delivery needle 2010 used totreat an area of interest 2002 (e.g., a nodule, tumor, lesion). Usedalone, a delivery needle 2010 (or other single-lumen needle) can havezone of efficacy 2050 within and/or around the area of interest 2002.For example, the delivery needle 2010 can be delivered to the area ofinterest 2002 and be inserted (e.g., piercably) into the area ofinterest 2002. A syringe or other fluid source (not shown) can beconnected to the proximal end 2015 of the delivery needle 2010 and canbe used to introduce a treatment substance (e.g., an ablative chemicalsolution) to the area of interest 2002 through the needle 2010. Thetreatment substance can travel through the distal end 2014 of the needle2010 to affect a zone of efficacy 2050. The zone of efficacy 2050 cangenerally comprise the area treated or otherwise affected by thetreatment substance.

As illustrated in FIG. 22B, the use of multiple internal needles 2040can increase the size of the zone of efficacy 2050 a compared to thezone of efficacy 2050 realized using a single-lumen, single needletreatment approach. For example, the delivery needle 2010 can benavigated to the area of interest 2002. The distal end 2014 of thedelivery needle 2010 can be inserted (e.g., piercably) into the site ofinterest 2002. The internal needles 2040 can be moved distally withrespect to the distal end 2014 of the delivery needle 2010 to furtherpenetrate the site of interest 2002. As described above, the internalneedles 2040 can be configured to flare outward from the distal end 2014of the delivery needle 2010 as the internal needles 2040 are advancedout of the delivery needle 2010 in the distal direction. A syringe orother fluid source can be connected to the proximal end of the internalneedles 2040 and/or flexible tube 2030 and can be used to introduce atreatment substance (e.g., an ablative chemical solution) to the area ofinterest 2002 through the internal needles 2040. In some embodiments,the treatment substance is ethanol, which can be used to treat and/ordestroy tumors. The treatment substance can travel through the cutfeatures 2042 and/or distal aperture 2044 to disperse the treatmentsubstance and create a zone of efficacy 2050 a that can be greater insize than the zone of efficacy 2050 realized using a single lumen,single needle treatment approach.

Although this invention has been disclosed in the context of certainembodiments and examples, those skilled in the art will understand thatthe present invention extends beyond the specifically disclosedembodiments to other alternative embodiments and/or uses of theinvention and obvious modifications and equivalents thereof. Inaddition, while several variations of the invention have been shown anddescribed in detail, other modifications, which are within the scope ofthis invention, will be readily apparent to those of skill in the artbased upon this disclosure. It is also contemplated that variouscombinations or sub-combinations of the specific features and aspects ofthe embodiments may be made and still fall within the scope of theinvention. It should be understood that various features and aspects ofthe disclosed embodiments can be combined with, or substituted for, oneanother in order to form varying modes or embodiments of the disclosedinvention. Thus, it is intended that the scope of the present inventionherein disclosed should not be limited by the particular disclosedembodiments described above.

What is claimed is:
 1. A needle assembly for delivery of a treatmentsubstance to a site within the body, the needle assembly comprising: adelivery needle defining a delivery lumen and having a delivery needlewall, a proximal end, and a distal end, the delivery needle wall havingone or more cut patterns to increase the flexibility of the deliveryneedle; a plurality of internal needles, each internal needle definingan internal needle lumen and having an internal needle wall, a proximalend, and a distal end, the plurality of needles configured to transitionbetween a contracted position and an expanded position; and a treatmentsubstance source in fluid communication with the internal needle lumensof the plurality of internal needles; wherein each of the plurality ofinternal needles is configured to extend in a distal direction and flareoutward from the distal end of the delivery needle when in the expandedposition; and wherein the plurality of internal needles are housedwithin the delivery lumen when in the contracted position.
 2. The needleassembly of claim 1, wherein an internal surface of the delivery needlewall is coated with a substance configured to reduce or eliminate thelikelihood that the internal needles will stick to or catch on thedelivery needle wall when the internal needles are transitioned betweenthe contracted position and the expanded position.
 3. The needleassembly of claim 1, wherein the delivery needle is coated on an outsidesurface with quick clotting features, cauterizing features, or both. 4.The needle assembly claim 2, wherein the internal surface of thedelivery needle wall includes one oe more cut features, the one or morecut features facilitating fluid communication between the internalneedle lumen and an exterior of the internal needles.
 5. The needleassembly of claim 4, wherein the needle assembly further comprises aflexible shaft having a distal end and a proximal end, the distal end ofthe flexible shaft coupled with the proximal ends of the internalneedles.
 6. The needle assembly of claim 1, wherein the needle assemblycomprises three internal needles.
 7. The needle assembly of claim 6,wherein each of the internal needles has a distal aperture in fluidcommunication with the internal needle lumen.
 8. The needle assembly ofclaim 1, wherein each of the distal ends of the internal needles aresharpened.
 9. The needle assembly of claim 8, wherein each of the distalends of the internal needles form a continuous beveled surface, whereinthe angle changes continuously along the bevel.
 10. The needle assemblyof claim 1, wherein the distal end of the delivery needle is sharpened.11. The needle assembly of claim 10, wherein the distal end of thedelivery needle forms a continuous beveled surface, wherein the anglechanges continuously along the bevel.
 12. The needle assembly of claim1, wherein the needle assembly further comprises a connection to asuction source, a steering mechanism, or both.
 13. A multi-lumencatheter assembly, comprising: a biopsy needle contained within onelumen; an ultrasound probe contained within a second lumen; and amechanism for adjusting the angle of the distal tip of the biopsyneedle, comprising one or more steering wires.
 14. The needle assemblyof claim 13, wherein the one or more steering wires is a bowden wire.15. A method of obtaining a tissue sample, comprising: inserting aneedle assembly in a bronchoscope; advancing a one or more flexibleneedles through a distal tip of the needle assembly; visualizing the tipposition with the aid of one or more signature markers; and manipulatinga position of the distal tip to optimally obtain the tissue sample.